Expired Study
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Boynton Beach, Florida 33437


Purpose:

A randomized, double-blind, placebo controlled study to assess the safety and effectiveness of a novel oral natural extract to improve the appearance of the skin of patients with senile purpura.


Criteria:

Inclusion Criteria: - Patients with evidence of purpura on physical exam Exclusion Criteria: - Preexisting condition that would not allow the patients to take oral calcium supplement


NCT ID:

NCT01183910


Primary Contact:

Principal Investigator
JOSHUA M BERLIN, MD
STUDY PROTOCOL, INC


Backup Contact:

N/A


Location Contact:

Boynton Beach, Florida 33437
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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